CO5140077A1 - STABLE INSOLUBLE COMPLEX IN WATER, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN IT AND METHODS FOR PREPARATION. . - Google Patents

STABLE INSOLUBLE COMPLEX IN WATER, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN IT AND METHODS FOR PREPARATION. .

Info

Publication number
CO5140077A1
CO5140077A1 CO99059117A CO99059117A CO5140077A1 CO 5140077 A1 CO5140077 A1 CO 5140077A1 CO 99059117 A CO99059117 A CO 99059117A CO 99059117 A CO99059117 A CO 99059117A CO 5140077 A1 CO5140077 A1 CO 5140077A1
Authority
CO
Colombia
Prior art keywords
weight
active compound
water insoluble
polymer
ionic polymer
Prior art date
Application number
CO99059117A
Other languages
Spanish (es)
Inventor
Antonio A Albano
Phuapradit Wantasnee
K Sandhu Harpreet
Hargovindas Shah Navnit
Original Assignee
Hoffmann La Roche
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=26798138&utm_source=***_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CO5140077(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Hoffmann La Roche filed Critical Hoffmann La Roche
Publication of CO5140077A1 publication Critical patent/CO5140077A1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/14Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/141Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
    • A61K9/146Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular compounds
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/51Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent
    • A61K47/56Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors

Abstract

Un complejo insoluble en agua que comprende al menos 20% en peso de un polímero iónico insoluble en agua que tiene un peso molecular superior a 80.000 D (1.32 x 10-19 g) y una temperatura de transición vítrea igual o superior a 50° C, y de 0.1 a 80% en peso de un compuesto activo estable y, amorfo que tiene una solubilidad acuosa inferior a 1 mg/ml.Un método para la preparación de un complejo insoluble en agua compuesto de al menos un 20% en peso de un polímero iónico que tiene un peso molecular superior a 80.000 D (1.32 x 10-19 g) y una temperatura de transición vítrea igual o superior a 50° C y, de 0.1 a 80% en peso de un compuesto activo estable y amorfo, preparado mediante: (a) la fusión conjunta del compuesto terapéuticamente activo y el polímero iónico; y(b) enfriamiento de la mezcla resultante del paso (a).Una composición farmacéutica que comprende un complejo insoluble en agua compuesto de al menos 20% en peso de un polímero iónico insoluble en agua que tiene un peso molecular superior a 80.000 D (1.32 x 10-19 g) y una temperatura de transición vítrea igual o superior a 50° C, de 0.1 a 80% en peso de un compuesto activo que tiene una solubilidad acuosa inferior a 1 mg/ml, y un soporte.2Un método para la preparación de una composición farmacéutica que comprende un complejo insoluble en agua compuesto de al menos un 20% en peso de un polímero iónico insoluble en agua que tiene un peso molecular superior a 80.000 D (1.32 x 10-19 g) y una temperatura de transición vítrea igual o superior a 50° C y, de 0.1 a 80% en peso de un compuesto activo que tiene una solubilidad acuosa inferior a 1 mg/ml, que comprende:(a) la disolución del compuesto terapéuticamente activo y el polímero iónico en un disolvente orgánico que provee buena solubilidad para ambos el compuesto activo y el polímero;(b) la puesta en contacto de la solución del paso (a) con una solución acuosa a un pH en el cual el polímero iónico es escasamente soluble, con lo cual tiene lugar la microprecipitación del compuesto terapéuticamente activo y el polímero iónico en forma de un complejo compuesto/polímero;(c) la mezcla del complejo compuesto/polímero del paso (b) con un soporte y/o ingredientes adicionales convencionales.A water insoluble complex comprising at least 20% by weight of a water insoluble ionic polymer having a molecular weight greater than 80,000 D (1.32 x 10-19 g) and a glass transition temperature equal to or greater than 50 ° C , and from 0.1 to 80% by weight of a stable and amorphous active compound having an aqueous solubility of less than 1 mg / ml. A method for the preparation of a water insoluble complex composed of at least 20% by weight of an ionic polymer having a molecular weight greater than 80,000 D (1.32 x 10-19 g) and a glass transition temperature equal to or greater than 50 ° C and 0.1 to 80% by weight of a stable and amorphous active compound, prepared by: (a) the joint fusion of the therapeutically active compound and the ionic polymer; and (b) cooling the mixture resulting from step (a). A pharmaceutical composition comprising a water insoluble complex composed of at least 20% by weight of a water insoluble ionic polymer having a molecular weight greater than 80,000 D ( 1.32 x 10-19 g) and a glass transition temperature equal to or greater than 50 ° C, from 0.1 to 80% by weight of an active compound having an aqueous solubility of less than 1 mg / ml, and a support.2 A method for the preparation of a pharmaceutical composition comprising a water insoluble complex composed of at least 20% by weight of a water insoluble ionic polymer having a molecular weight greater than 80,000 D (1.32 x 10-19 g) and a temperature of glass transition equal to or greater than 50 ° C and, from 0.1 to 80% by weight of an active compound having an aqueous solubility of less than 1 mg / ml, comprising: (a) the solution of the therapeutically active compound and the polymer ionic in an organic solvent that pro The active compound and the polymer have good solubility for both; (b) the contacting of the solution of step (a) with an aqueous solution at a pH in which the ionic polymer is sparingly soluble, whereby the microprecipitation of the therapeutically active compound and the ionic polymer in the form of a compound / polymer complex; (c) mixing the compound / polymer complex of step (b) with a conventional additional support and / or ingredients.

CO99059117A 1998-09-22 1999-09-17 STABLE INSOLUBLE COMPLEX IN WATER, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN IT AND METHODS FOR PREPARATION. . CO5140077A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US10133698P 1998-09-22 1998-09-22
US13653199P 1999-05-28 1999-05-28

Publications (1)

Publication Number Publication Date
CO5140077A1 true CO5140077A1 (en) 2002-03-22

Family

ID=26798138

Family Applications (1)

Application Number Title Priority Date Filing Date
CO99059117A CO5140077A1 (en) 1998-09-22 1999-09-17 STABLE INSOLUBLE COMPLEX IN WATER, PHARMACEUTICAL COMPOSITIONS THAT CONTAIN IT AND METHODS FOR PREPARATION. .

Country Status (33)

Country Link
US (1) US6350786B1 (en)
EP (1) EP0988863B2 (en)
JP (5) JP2000095708A (en)
KR (1) KR100362019B1 (en)
CN (1) CN1201821C (en)
AR (2) AR022096A1 (en)
AT (1) ATE265232T1 (en)
AU (1) AU770745B2 (en)
BR (1) BR9904283A (en)
CA (1) CA2282906C (en)
CO (1) CO5140077A1 (en)
CZ (1) CZ300215B6 (en)
DE (1) DE69916733T3 (en)
DK (1) DK0988863T4 (en)
ES (1) ES2218918T5 (en)
HK (1) HK1026632A1 (en)
HR (1) HRP990287B1 (en)
HU (1) HU228341B1 (en)
ID (1) ID24034A (en)
IL (1) IL131957A (en)
MA (1) MA26692A1 (en)
MY (1) MY124377A (en)
NO (1) NO326928B1 (en)
NZ (1) NZ337884A (en)
PE (1) PE20001049A1 (en)
PL (1) PL202757B1 (en)
PT (1) PT988863E (en)
RS (1) RS50193B (en)
RU (1) RU2240827C2 (en)
SG (1) SG97131A1 (en)
SI (1) SI0988863T2 (en)
TR (1) TR199902324A3 (en)
TW (1) TWI234465B (en)

Families Citing this family (85)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2307482T3 (en) 1999-02-10 2008-12-01 Pfizer Products Inc. SOLID PHARMACEUTICAL DISPERSIONS.
US6440959B1 (en) 1999-04-21 2002-08-27 Hoffman-La Roche Inc. Pyrazolobenzodiazepines
AR033651A1 (en) * 1999-10-01 2004-01-07 Hoffmann La Roche DERIVATIVES OF PYRIMIDINE-2,4,6-TRIONA, PHARMACEUTICAL COMPOSITIONS CONTAINING THESE COMPOUNDS AND THE USE OF THEM FOR THE MANUFACTURE OF A MEDICINAL PRODUCT
US6313143B1 (en) * 1999-12-16 2001-11-06 Hoffmann-La Roche Inc. Substituted pyrroles
JP4786113B2 (en) * 2000-05-16 2011-10-05 オーソーマクニール ファーマシューティカル, インコーポレイテッド Method for coating medical devices using supercritical carbon dioxide
US6482847B2 (en) 2000-10-03 2002-11-19 Hoffmann-La Roche Inc. Amorphous form of cell cycle inhibitor having improved solubility and bioavailability
US6469179B1 (en) 2000-10-03 2002-10-22 Hoffmann-La Roche Inc. Amorphous form of cell cycle inhibitor having improved solubility and bioavailability
US8067032B2 (en) 2000-12-22 2011-11-29 Baxter International Inc. Method for preparing submicron particles of antineoplastic agents
US9700866B2 (en) 2000-12-22 2017-07-11 Baxter International Inc. Surfactant systems for delivery of organic compounds
US20050048126A1 (en) 2000-12-22 2005-03-03 Barrett Rabinow Formulation to render an antimicrobial drug potent against organisms normally considered to be resistant to the drug
US6548531B2 (en) 2001-02-09 2003-04-15 Hoffmann-La Roche Inc. Method for cancer therapy
US6716845B2 (en) 2001-03-30 2004-04-06 Hoffmann-La Roche Inc. Barbituric acid derivatives
EP1401404B1 (en) * 2001-05-30 2008-04-16 Csir Method of encapsulating an active substance
US20030044514A1 (en) * 2001-06-13 2003-03-06 Richard Robert E. Using supercritical fluids to infuse therapeutic on a medical device
WO2002102373A1 (en) * 2001-06-15 2002-12-27 F. Hoffmann-La Roche Ag Method for administration of cancer therapeutic
ATE444060T1 (en) 2001-06-22 2009-10-15 Pfizer Prod Inc PHARMACEUTICAL COMPOSITIONS CONTAINING DISPERSIONS OF MEDICINAL SUBSTANCES AND NEUTRAL POLYMERS
DE60237602D1 (en) 2001-06-22 2010-10-21 Bend Res Inc PHARMACEUTICAL COMPOSITION CONTAINING HEAVY SOLUBLE AND ACIDIC TOXIC SUBSTANCES AND NEUTRALIZED ANIONIC POLYMERS
US20060003012A9 (en) 2001-09-26 2006-01-05 Sean Brynjelsen Preparation of submicron solid particle suspensions by sonication of multiphase systems
AU2002337692B2 (en) 2001-09-26 2007-09-13 Baxter International Inc. Preparation of submicron sized nanoparticles via dispersion and solvent or liquid phase removal
US20030139373A1 (en) * 2001-11-20 2003-07-24 Breimer Lars Holger Method for cancer therapy
CN1309370C (en) * 2002-02-01 2007-04-11 辉瑞产品公司 Method for making homogeneous spray-dried solid amorphous drug dispersions utilizing modified spray-drying apparatus
WO2004014342A1 (en) 2002-08-12 2004-02-19 Pfizer Products Inc. Pharmaceutical compositions of semi-ordered drugs and polymers
DE10351087A1 (en) * 2003-10-31 2005-05-25 Bayer Technology Services Gmbh Solid active ingredient formulation
JP4947482B2 (en) * 2003-11-14 2012-06-06 味の素株式会社 Sustained release oral administration of phenylalanine derivatives
CN101664411A (en) 2003-11-14 2010-03-10 味之素株式会社 Solid dispersion or medicinal solid dispersion preparation of phenylalanine derivative
KR100771411B1 (en) * 2004-04-01 2007-10-30 에프. 호프만-라 로슈 아게 Cyclodextrin inclusions complexes of pyrimidine-2,4,6-triones
AR049915A1 (en) * 2004-06-14 2006-09-13 Anacor Pharmaceuticals Inc COMPOUNDS WITH BORO CONTENT AND METHODS OF USE OF THE SAME
WO2006062980A2 (en) * 2004-12-07 2006-06-15 Nektar Therapeutics Stable non-crystalline formulation comprising tiagabine
CN101115469A (en) * 2004-12-28 2008-01-30 卫材R&D管理有限公司 Quick disintegration tablet and method of producing the same
US8604055B2 (en) 2004-12-31 2013-12-10 Dr. Reddy's Laboratories Ltd. Substituted benzylamino quinolines as cholesterol ester-transfer protein inhibitors
KR101238525B1 (en) * 2004-12-31 2013-02-28 레디 유에스 테라퓨틱스 인코포레이티드 Novel benzylamine derivatives as cetp inhibitors
EP1690528A1 (en) * 2005-02-11 2006-08-16 Abbott GmbH & Co. KG Process for the preparation of dosage forms comprising a solid dispersion of a microcrystalline active agent
EP1885338A1 (en) * 2005-05-19 2008-02-13 Pfizer, Inc. Pharmaceutical compostions comprising an amorphous form of a vegf-r inhibitor
EP1767194A1 (en) * 2005-06-09 2007-03-28 Helm AG Process for the preparation of adsorbates of drospirenone
BRPI0611863B1 (en) * 2005-06-22 2021-11-23 Plexxikon, Inc COMPOUND, AS WELL AS COMPOSITION AND KIT COMPRISING THE SAME, INTERMEDIATE COMPOUND IN THE PREPARATION OF THE SAME, METHOD FOR TREATMENT AND USE OF THE SAME
US20080031944A1 (en) * 2006-08-04 2008-02-07 Cima Labs Inc. Stabilization of lorazepam
BRPI0714265A2 (en) * 2006-08-10 2013-04-16 Cipla Ltd solid oral composition, process for preparing a solid oral composition, use of a composition and method for treating HIV
US20080107725A1 (en) * 2006-10-13 2008-05-08 Albano Antonio A Pharmaceutical Solid Dosage Forms Comprising Amorphous Compounds Micro-Embedded in Ionic Water-Insoluble Polymers
WO2008063888A2 (en) 2006-11-22 2008-05-29 Plexxikon, Inc. Compounds modulating c-fms and/or c-kit activity and uses therefor
WO2008079909A1 (en) * 2006-12-21 2008-07-03 Plexxikon, Inc. Pyrrolo [2,3-b] pyridines as kinase modulators
PE20121126A1 (en) * 2006-12-21 2012-08-24 Plexxikon Inc PIRROLO [2,3-B] PYRIDINES COMPOUNDS AS KINASE MODULATORS
WO2008081829A1 (en) 2006-12-27 2008-07-10 Astellas Pharma Inc. Aminoalkylmethacrylate copolymer e for maintaining solubility of poorly water-soluble drug
CN101702878B (en) * 2007-05-11 2012-11-28 弗·哈夫曼-拉罗切有限公司 Pharmaceutical compositions for poorly soluble drugs
US8426467B2 (en) 2007-05-22 2013-04-23 Baxter International Inc. Colored esmolol concentrate
US8722736B2 (en) 2007-05-22 2014-05-13 Baxter International Inc. Multi-dose concentrate esmolol with benzyl alcohol
EP1997479A1 (en) * 2007-05-31 2008-12-03 Helm AG Stabilized amorphous candesartan cilexetil compositions for oral administration
EP2170830B1 (en) 2007-07-17 2014-10-15 Plexxikon, Inc. 2-FLUORO-BENZENESULFONAMIDE COMPOUNDS AS Raf KINASE MODULATORS
EP2214635A1 (en) * 2007-10-19 2010-08-11 Purdue Research Foundation Solid formulations of crystalline compounds
US7794750B2 (en) * 2008-06-20 2010-09-14 Mutual Pharmaceutical Company, Inc. Controlled-release formulations, method of manufacture, and use thereof
US8632805B2 (en) * 2008-06-20 2014-01-21 Mutual Pharmaceutical Company, Inc. Controlled-release formulations, method of manufacture, and use thereof
WO2010044842A1 (en) * 2008-10-16 2010-04-22 University Of Tennessee Research Foundation Tamper resistant oral dosage forms containing an embolizing agent
KR20100073454A (en) * 2008-12-23 2010-07-01 국립암센터 Novel pyrazolodiazepine compound as an transglutaminase inhibitor, the preparation method thereof and a composition containing the same
MY172424A (en) * 2009-04-03 2019-11-25 Hoffmann La Roche Propane- i-sulfonic acid {3- (4-chloro-phenyl)-1h-pyrrolo [2, 3-b] pyridine-3-carconyl] -2, 4-difluoro-phenyl} -amide compositions and uses thereof
US8329724B2 (en) 2009-08-03 2012-12-11 Hoffmann-La Roche Inc. Process for the manufacture of pharmaceutically active compounds
BR112012012156A2 (en) 2009-11-06 2015-09-08 Plexxikon Inc compounds and methods for kinase modulation, and indications for this
KR20130126451A (en) * 2010-05-31 2013-11-20 아스테라스 세이야쿠 가부시키가이샤 Solid dispersion comprising triazole compound
TR201816421T4 (en) 2011-02-07 2018-11-21 Plexxikon Inc Compounds and methods for kinase modulation and their indications.
CN103391769A (en) 2011-02-17 2013-11-13 霍夫曼-拉罗奇有限公司 A process for controlled crystallization of an active pharmaceutical ingredient from supercooled liquid state by hot melt extrusion
AR085279A1 (en) 2011-02-21 2013-09-18 Plexxikon Inc SOLID FORMS OF {3- [5- (4-CHLORINE-PHENYL) -1H-PIRROLO [2,3-B] PIRIDINA-3-CARBONIL] -2,4-DIFLUOR-PHENIL} -AMIDE OF PROPANE ACID-1- SULFONIC
US9199967B2 (en) 2011-08-18 2015-12-01 Dr. Reddy's Laboratories Ltd. Substituted heterocyclic amine compounds as cholestryl ester-transfer protein (CETP) inhibitors
WO2013037396A1 (en) * 2011-09-12 2013-03-21 Bioneer A/S Solution of polymer in api for a solid dosage form
CA2850022C (en) 2011-09-27 2018-05-01 Dr. Reddy's Laboratories, Ltd. 5 - benzylaminomethyl - 6 - aminopyrazolo [3,4-b] pyridine derivatives as cholesteryl ester-transfer protein (cetp) inhibitors useful for the treatment of atherosclerosis
CN108498465B (en) * 2011-10-14 2022-05-17 阵列生物制药公司 Solid dispersions of an ErbB2(HER2) inhibitor
SI2827900T1 (en) 2012-03-23 2018-06-29 Array Biopharma, Inc. Amorphous solid dispersion for use in the treatment of brain cancer
US20140128431A1 (en) 2012-04-03 2014-05-08 Hoffmann-Laroche Inc. Pharmaceutical composition with improved bioavailability, safety and tolerability
EP2649989B1 (en) 2012-04-13 2017-10-18 King Saud University Method for preparing a solid dispersion, solid dispersion obtained thereby and use thereof
US9150570B2 (en) 2012-05-31 2015-10-06 Plexxikon Inc. Synthesis of heterocyclic compounds
JO3339B1 (en) * 2012-09-11 2019-03-13 Shanghai Inst Pharmaceutical Ind Stabilised amorphous form of agomelatine, a process for its preparation and pharmaceutical compositions containing it
RU2015123632A (en) 2012-11-19 2017-01-10 Др. Редди'С Лабораторис Лтд. PHARMACEUTICAL COMPOSITIONS OF CETR INHIBITORS
CN105007899A (en) * 2012-12-20 2015-10-28 卡希夫制药有限责任公司 Orally disintegrating tablet formulation for enhanced bioavailability
MY192032A (en) 2013-01-22 2022-07-24 Hoffmann La Roche Pharmaceutical composition with improved bioavailability
TWI615157B (en) 2013-02-06 2018-02-21 大塚製藥股份有限公司 Solid dispersion comprising amorphous cilostazol
US20160213575A1 (en) * 2013-09-11 2016-07-28 3M Innovative Properties Company Coating compositions, dental structures thereof and methods for generating contrast
US20160303102A1 (en) * 2013-12-05 2016-10-20 Alrise Biosystems Gmbh Process for the production of drug formulations for oral administration
PT107846B (en) * 2014-08-01 2019-03-22 Hovione Farm S A Production of Amorphous Solid Dispersion Nanoparticles by Controlled Co-Precipitation
BR112017025739A2 (en) * 2015-05-29 2018-08-07 Sun Pharmaceutical Ind Ltd isotretinoin oral pharmaceutical composition having increased bioavailability, process for preparing it and method of treatment
EP3447056A4 (en) 2016-12-13 2019-09-18 Nanjing Transthera Biosciences Co. Ltd. Multi-kinase inhibitor compound, and crystal form and use thereof
KR20200014298A (en) 2017-04-28 2020-02-10 시애틀 지네틱스, 인크. Treatment of HER2-positive cancer
KR102082775B1 (en) * 2017-05-02 2020-02-28 주식회사 삼양바이오팜 Formulation with enhanced water solubility and bioavailability
RU2725879C2 (en) * 2018-07-26 2020-07-07 Федеральное государственное бюджетное образовательное учреждение высшего образования "Казанский Государственный медицинский университет" Министерства здравоохранения Российской Федерации Interpolymer carrier for oral systems of controlled delivery of active pharmaceutical ingredients
JP2022509965A (en) 2018-12-03 2022-01-25 ハー・ルンドベック・アクチエゼルスカベット 4-((1R, 3S) -6-chloro-3-phenyl-2,3-dihydro-1H-inden-1-yl) -1,2,2-trimethylpiperazine and 4-((1R, 3S)- Prodrug of 6-chloro-3- (phenyl-d5) -2,3-dihydro-1H-indene-1-yl) -2,2-dimethyl-1- (methyl-d3) piperazine
EP4093379A1 (en) 2020-01-24 2022-11-30 Nanocopoeia LLC Amorphous solid dispersions of dasatinib and uses thereof
IL295007A (en) 2020-01-31 2022-09-01 Nanocopoeia Llc Amorphous nilotinib microparticles and uses thereof
KR20220129628A (en) 2020-03-03 2022-09-23 데쿠세리아루즈 가부시키가이샤 Method for manufacturing an image display device
EP4142699A1 (en) 2020-04-30 2023-03-08 Nanocopoeia LLC Orally disintegrating tablet comprising amorphous solid dispersion of nilotinib

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS51118816A (en) * 1975-04-08 1976-10-19 Meiji Seika Kaisha Ltd A process for stabilizing non-crystalloidal solid
US4344934A (en) * 1978-11-20 1982-08-17 American Home Products Corporation Therapeutic compositions with enhanced bioavailability
FI864812A (en) * 1985-11-27 1987-05-28 Syntex Inc FOERFARANDE FOER FRAMSTAELLNING AV AMORFA BENSIMIDAZOLDERIVAT.
CZ280738B6 (en) * 1988-02-10 1996-04-17 F. Hoffmann - La Roche And Co., Aktiengesellschaft Substituted pyrroles, their use for preparing medicaments and medicaments based thereon
JP2528706B2 (en) 1988-05-30 1996-08-28 ゼリア新薬工業株式会社 Pharmaceutical composition of dihydropyridine compound
USRE36736E (en) 1989-02-06 2000-06-13 Hoffman-La Roche Inc. Substituted pyrroles
JPH0729926B2 (en) 1989-07-25 1995-04-05 大塚製薬株式会社 Composition for easily absorbable preparations
US5399363A (en) 1991-01-25 1995-03-21 Eastman Kodak Company Surface modified anticancer nanoparticles
AU1537292A (en) 1991-04-16 1992-11-17 Nippon Shinyaku Co. Ltd. Method of manufacturing solid dispersion
US5281420A (en) 1992-05-19 1994-01-25 The Procter & Gamble Company Solid dispersion compositions of tebufelone
TW493991B (en) 1995-05-08 2002-07-11 Novartis Ag Pharmaceutical composition for oral administration of active agent having low water solubility and process for preparation of the same
GB9511220D0 (en) 1995-06-02 1995-07-26 Glaxo Group Ltd Solid dispersions
ATE240734T1 (en) * 1995-07-26 2003-06-15 Kyowa Hakko Kogyo Kk PREPARATION OF XANTHINDERIVATES AS A SOLID DISPERSION
AU7106996A (en) 1995-09-07 1997-03-27 Fuisz Technologies Ltd. System for rendering substantially non-dissoluble bio-affecting agents bio-available
DE19548624A1 (en) 1995-12-23 1997-06-26 Boehringer Mannheim Gmbh New barbituric acid derivatives, processes for their preparation and medicaments containing these compounds
JPH09208459A (en) * 1996-02-07 1997-08-12 Eisai Co Ltd Preparation improved in solubility
JP3737518B2 (en) 1996-03-12 2006-01-18 ピージー−ティーエックスエル カンパニー, エル.ピー. Water-soluble paclitaxel prodrug
JP2000514057A (en) * 1996-06-28 2000-10-24 シェーリング コーポレイション Solid solution of antifungal agent with enhanced bioavailability
PE91598A1 (en) 1996-07-29 1998-12-24 Hoffmann La Roche SUBSTITUTED PYRROLES
US6229011B1 (en) 1997-08-22 2001-05-08 Hoffman-La Roche Inc. N-aroylphenylalanine derivative VCAM-1 inhibitors
CZ299068B6 (en) 1998-03-17 2008-04-16 F. Hoffmann-La Roche Ag Substituted bisindolylmaleimide and pharmaceutical composition containing thereof

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